ライフサイエンスコーパス: absorption band

1 and 950cm(-1) (glucose, fructose and sucrose absorption bands).

2 ee ligand absorption and increase of complex absorption band.

3 hromic shift of its lowest energy electronic absorption band.

4 optical intervalence charge-transfer (IVCT) absorption band.

5 y tuning the pump laser into the gain medium absorption band.

6 t light scatters around the nanogold plasmon absorption band.

7 y 5-nm red shift of the long wavelength Q(y) absorption band.

8 the strength of the lowest-energy two-photon absorption band.

9 approximately 30 nm blue shift of the dimer absorption band.

10 ions upon NIR excitation at 980 nm in the Yb absorption band.

11 escence from the blue to the red side of the absorption band.

12 e--after optical excitation tuned to the CDW absorption band.

13 es weaker than those of the strongest mid-IR absorption bands.

14 a separation of the E and Z isomers' n-->pi* absorption bands.

15 o a second excited state with two CN-stretch absorption bands.

16 ong electronic transitions of photosynthetic absorption bands.

17 essively red-shifted primary charge-transfer absorption bands.

18 nent spectra with overlapped or superimposed absorption bands.

19 dders revealed both polaron and intervalence absorption bands.

20 ing agents with multiple and broadly tunable absorption bands.

21 lexes producing new red-shifted emission and absorption bands.

22 ole in determining the line shape of such CT absorption bands.

23 he molecular origins of their distinctive IR absorption bands.

24 -unsaturated ketones are split into distinct absorption bands.

25 liquid solutions for different emission and absorption bands.

26 e and layer can substantially deviate around absorption bands.

27 utions of the IL used in this study show two absorption bands.

28 to the absolute positions of the water vapor absorption bands.

29 ndow corresponding to the protein Amide I/II absorption bands.

30 g. by means of studying characteristic water absorption bands.

31 Upon irradiation in the tail of the absorption bands (490 nm), both the isomers exhibit more

32 iochlorophylls), with a strong near-infrared absorption band (707-751 nm).

33 roposed that in S65T/H148D, the red shift of absorption band A and the ultrafast appearance of green

34 that hypochromism induced in the tryptophan absorption band, a ground-state effect, is a significant

35 and the variant S65T/H148D each exhibit two absorption bands, A and B, which are associated with the

36 ssignment of the observed MCD and electronic absorption bands, a detailed understanding of the metal-

37 The lowest Q(y) state in absorption band (A1) is characterized by an electron-pho

38 phan oxidation products exhibited a distinct absorption band above 280 nm shifted to the longer wavel

39 proteins give rise to nine characteristic IR absorption bands (amides A, B and I-VII).

40 They are also characterized by a wide absorption band and a narrow emission band, which makes

41 show this species to have a distinct visible absorption band and a transition moment that we suggest

42 rized by a 1017 nm bacteriochlorophyll anion absorption band and decays by charge recombination with

43 ystine was quantitated using its 1296 cm(-1) absorption band and levels matched with parallel measure

44 Spectral overlap between the azobenzene absorption band and plasmonic resonances of silver nanow

45 engths corresponding to the hemoglobin Soret absorption band and to the absorption bands of the dyes

46 avelengths within both the H and J aggregate absorption bands and are imaged on the surface of silica

47 rmined from the intervalence charge-transfer absorption bands and from electronic structure calculati

48 osition produces a bathochromic shift of all absorption bands and makes alpha and beta bands equal as

49 s have enhanced and bathochromically shifted absorption bands and much better solubility in organic s

50 lasmons allow ultrasensitive measurements of absorption bands and surface phonon modes in angstrom-th

51 the absorption edge, appearance of a new IR absorption band, and Auger quenching of the excitonic ph

52 idation potential, bathochromic shift of the absorption band, and minimization of the emission quantu

53 gap between their first and second excitonic absorption bands, and this narrowing effect is size-depe

54 )18 clusters exhibit multiple molecular-like absorption bands, and we find the results are in good co

55 New UV/Vis absorption bands appear upon addition of diazabicyclooct

56 Intervalence absorption bands appearing in the diagnostic near-IR reg

57 A new visible absorption band appears in the presence of polar solvent

58 For one of the anionic guests, a visible absorption band appears upon host-guest formation with t

59 de aerosol substrates exhibits a red-shifted absorption band ( approximately 450-650 nm) consistent w

60 profiles in resonance with the lowest energy absorption band are measured.

61 to all of the excitation profiles and to the absorption band are obtained using one set of excited-st

62 The resulting long wavelength excitation/absorption bands are a synergistic property of the compo

63 ET barriers evaluated from the intervalence absorption bands are also quantitatively verified by the

64 quaraine (SQ) donor molecules with different absorption bands are blended together for better coverag

65 hat the vibrationally resolved lowest-energy absorption bands are characterized by a transition dipol

66 nd the direction of electron oscillations in absorption bands are discussed.

67 erization, and the relative positions of all absorption bands are found to be in agreement with the e

68 2), Broad, "dimer" absorption bands are observed for both P700(+) and P740(

69 n the colloids are in proximity, the plasmon absorption bands are often perturbed.

70 ults for Mn-depleted PS II, multiple near-IR absorption bands are resolved in the light-minus-dark di

71 , and it has long been a mystery why Vesta's absorption bands are so strong.

72 sample using a hypsochromic shift of another absorption band around 340 nm that is independent of the

73 inating ruthenium to the thiophenes is a new absorption band around 470 nm.

74 ecifically, it exhibits a blue-shifted broad absorption band around 500 nm and a rR spectrum with a n

75 The UV-vis spectrum of 1 shows a broad absorption band around 550 nm that is assigned to a char

76 ternation vibrational mode, treating the GFP absorption band as an intervalence charge transfer band.

77 tions of the location of seven near-infrared absorption bands as functions of temperature 5-50 degree

78 nd UV-vis detection allows observation of an absorption band assigned to singlet 2-oxocyclohexa-3,5-d

79 the dimer radical cation was replaced by an absorption band assigned to the (alpha-thio)benzyl catio

80 nges and the significance of charge-transfer absorption bands associated with the reduction of FAD by

81 s (ethanol or tert-butanol) identified by an absorption band at 1694 cm(-1); however, we find no evid

82 sor of this reactive site with an associated absorption band at 29,000 cm(-1).

83 AMAM dendrimer results in a strong, distinct absorption band at 300 nm, making UV-vis spectrophotomet

84 on spectrum shows near-zero overlap with the absorption band at 325 nm.

85 In the presence of 4-hydroxypyridine, a new absorption band at 338 nm, assigned to the alpha-aminoac

86 were accompanied by the appearance of a new absorption band at 376 nm in the UV-vis spectrum consist

87 broad metal-to-ligand charge transfer (MLCT) absorption band at 450 nm with epsilon = 1.7 x 10(4) M(-

88 o form brown carbon (BrC) with a distinctive absorption band at 505 nm.

89 f AMTr-AuNPs was changed into purple and the absorption band at 520 nm was decreased.

90 to take place, which produced a specific new absorption band at 600 nm for detection.

91 ical interactions, which give rise to an NIR absorption band at 900 nm, tend to play a crucial role i

92 In contrast, the energy of the absorption band at about 295 nm, designated as pi(CS) --

93 decrease in the magnitude of the UV-visible absorption band at approximately 400 nm that we attribut

94 perties with compounds showing a high-energy absorption band at ca. 270-290 nm and a low-energy band

95 window corresponding to the protein Amide A absorption band at dilution by a factor of 900 (0.034% w

96 tions of 1 in THF-d8 possess a strong UV-vis absorption band at lambda(max) approximately 640 nm.

97 the aggregate of DD-PTCDI shows a pronounced absorption band at the longer wavelength, whereas the ab

98 ized tryptophan residue exhibited a distinct absorption band at the maximum absorbance wavelength 335

99 The macrocycles showed one broad absorption band at ~553 nm with a shoulder peak at the h

100 AuAg nanohollows have an absorption band at ~630 nm, and slightly off-resonance 7

101 Two sharp absorption bands at 1418 cm(-1) and 3323 cm(-1) were att

102 ved IR (TRIR) spectroscopy as characteristic absorption bands at 1814, 2101, and 2038 cm-1, respectiv

103 tion of ciprofloxacin, PVD showed new UV-vis absorption bands at 252 and 321nm due to an internal cha

104 sis is colorless, but turns green with broad absorption bands at 430 and 680 nm after reconstitution

105 imonene SOA, both of which produced BrC with absorption bands at 475 and 505 nm, respectively.

106 On FdTt unfolding at alkaline pH, new absorption bands at 520 nm and 610 nm appear transiently

107 au = 333 ns, kobs = 3.0 x 106 M-1s-1) having absorption bands at 570 and 620 nm in CH3CN.

108 nm from carotenoids as well as smaller Q(y) absorption bands at 672 and 812 nm from chlorophyll a an

109 ynthesized Ar4TNPs exhibit remarkably strong absorption bands at 710-720 nm (epsilon approximately 20

110 These as-synthesized NCs exhibit absorption bands at around 590 nm (~2.1 eV) and 410 nm (

111 tylimide ring, exhibits the most red-shifted absorption band (at lambda(max) = 746 nm), the lowest fl

112 NikD exhibits an unusual long wavelength absorption band attributed to a charge transfer complex

113 ds, including a unique low-energy electronic absorption band, attributed to an IVCT-type transition t

114 however, exhibits an unusual long-wavelength absorption band, attributed to charge-transfer interacti

115 periments following excitation on the second absorption band (B-band) at around 201 nm.

116 We observe multiple absorption bands but no cross peaks in the 2D IR spectra

117 The polarons of F(3) and F(4) display sharp absorption bands, but for longer oligomers the bands bro

118 of excited states are characterized by a red absorption band (ca. 600 nm) assigned to Co 3d --> 3d or

119 as reflectivity and spectral position of the absorption band can be varied in situ within +/-0.5 V.

120 l results indicate that the bandwidth of the absorption bands can be controlled by changing the diele

121 y using mixtures of D(2)O and H(2)O, water's absorption bands can be made to be on-scale in transmiss

122 ngths beyond 800 nm, clearly outside the LWC absorption bands, can still induce photochemical charge

123 n around 1510 cm(-1) and a visible transient absorption band centered at 760 nm.

124 arge-transfer complex with a long-wavelength absorption band centered at 780 nm.

125 e asteroid Vesta has prominent near-infrared absorption bands characteristic of a range of pyroxenes,

126 FTIR of the coatings showed absorption bands characteristic of phosphate groups, and

127 d a 2-fold slower decay of the excited-state absorption bands compared to the monomer M (tau4,foldame

128 nd MEH-PPV oligomers, the calculated intense absorption bands converge at the longest wavelengths for

129 intensity of the resulting particle plasmon absorption bands correlates well with the redox characte

130 which displayed no enzymatic activity and no absorption band corresponding to an internal PLP-aldamin

131 The CO adduct of T67R/S92D shows two CO absorption bands corresponding to the A(1) and A(3) subs

132 The subpicosecond transient absorption bands decay may reflect rapid charge separati

133 The presence of two CN-stretch absorption bands demonstrates that this secondary excite

134 entally observed shifts in known chlorophyll absorption bands, demonstrating the predictive capabilit

135 n and had the same lifetime as the transient absorption band detected in the visible region, confirmi

136 However, the visible absorption band does not match that of the monomeric cat

137 ids are well known to display strong plasmon absorption bands due to electron oscillations induced by

138 at least one of the lower-energy electronic absorption bands (E(max) approximately 16300 cm(-1)) is

139 rgies below the band edge, whereas above the absorption band edge of hematite, the surface plasmon po

140 These aggregates exhibit a red-shifted absorption band, enhanced fluorescence emission, and an

141 Large red shifts of the UV/vis absorption bands evidence efficient incorporation of the

142 Both absorption bands exhibit a modest negative solvatochromi

143 The SPR absorption band exhibits an exceptional behavior: As siz

144 ded pentafulvenes feature intense electronic absorption bands, extending over the entire visible spec

145 ure is increased from low temperature, a new absorption band for the unfolded protein grows in and th

146 Compared to the wild type, the Qy absorption bands for BChl c in the mutant cells were nar

147 Weak CT absorption bands for D-A complexes occur at photon energ

148 stematically examined, and characteristic IR absorption bands for the corresponding N-trifluoromethan

149 The observed UV-visible absorption bands for the Fe(3+)-nitrile intermediate spe

150 H complex is 200 microM with charge-transfer absorption bands for the KMO(RED).l-Kyn.NADP(+) complex

151 dent response of the diagnostic intervalence absorption bands for the quantitative evaluation of the

152 ectra of glycosylated proteins show distinct absorption bands for the sugar moiety, the protein amide

153 of the molecules' dipole moments and J-type absorption band formation in thin films.

154 aid in the assignment of the intense near-UV absorption bands found for the oxoiron(IV) complexes wit

155 during nanowire growth by comparing nu(Ge-H) absorption bands from operando measurements (i.e., durin

156 redox difference spectroscopy has identified absorption bands from the COOH group of E107.

157 perimental results indicate that the amide I absorption band in D(2)O (i.e., amide I') attributable t

158 y the lack of a detectable 1-micrometer Fe2+ absorption band in high-spatial-resolution spectra of ma

159 ort here the observation of a giant-infrared-absorption band in reduced graphene oxide, arising from

160 (3)OC(6)H(4)CN(2)CH(3)) produced a transient absorption band in the 400-700 nm region.

161 the hypsochromic shift of the characteristic absorption band in the electronic spectra.

162 at the blue shift and increased width of the absorption band in the L135 mutants are due partly to ch

163 gths, matches well with the short-wavelength absorption band in the linear electronic spectrum and is

164 th flavins, and are characterized by a broad absorption band in the long wavelength region.

165 strong intramolecular charge transfer (ICT) absorption band in the near IR region.

166 ludes appearance of an intervalence transfer absorption band in the near IR spectrum of the photochem

167 st time by its diagnostic (charge-resonance) absorption band in the near-IR region.

168 ns prepared herein exhibit a long-wavelength absorption band in the range 707-759 nm, providing tunab

169 Each bacteriochlorin exhibits a Q(y) absorption band in the range of 720-772 nm.

170 denced by the concomitant formation of a new absorption band in the UV/vis spectrum at 390 nm.

171 Detailed analysis of 1[n] revealed a broad absorption band in the visible region with maxima at 540

172 This compound has a major absorption band in the visible wavelength region with a

173 attributed to chromium impurities and their absorption band in the yellow region of the visible ligh

174 ree polysaccharides showed typical saccharic absorption bands in FT-IR.

175 rspectral illumination to target chromophore absorption bands in the 900-1,300 nm wavelength range.

176 Each chlorin exhibits dominant absorption bands in the blue and the red region (lambda

177 Both modified starches reported absorption bands in the IR at 1566 and 1738 cm(-1), prop

178 The CO adduct of Ngb displays two CO absorption bands in the IR spectrum, referred to as N(3)

179 between chemicals with strongly overlapping absorption bands in the mid-infrared.

180 TBPs and TNPs possess powerful absorption bands in the near-infrared (lambda = 610-710

181 igh solubility and exhibit remarkably strong absorption bands in the near-infrared region (790-950 nm

182 these rectangles reveal intense, asymmetric absorption bands in the near-infrared region, assigned a

183 dimeric species are characterized by intense absorption bands in the near-IR region that are diagnost

184 ll possessing a high fluorophore brightness, absorption bands in the near-UV and visible part of the

185 chromic shifts in both the Soret and visible absorption bands in the presence of Cc and an absorption

186 ot have any influence on the position of the absorption bands in the spectra.

187 that of their pyrimidine counterparts, with absorption bands in the UV or visible region and the emi

188 All of the compounds have intense absorption bands in the UV region assigned into (1)(pi -

189 mation of anion-pai complexes showing strong absorption bands in the UV-vis range.

190 Their absorption bands in the vis region of the spectra are du

191 Theoretical calculations indicate that the absorption bands in the visible range can be tuned using

192 lorin, and BODIPY derivatives with different absorption bands in the visible region (503-668 nm) have

193 tense metal-to-ligand charge-transfer (MLCT) absorption bands in the visible region and room temperat

194 These compounds feature strong MLCT absorption bands in the visible region and strong red ph

195 The two outputs are the absorption bands in the visible region of the two colore

196 CYP3A4-Nanodiscs have absorption bands in the visible wavelength region, which

197 ut the lack of spectral data across telluric absorption bands in the wavelength region 2.5 to 2.9 mic

198 lecular orbitals that contribute to the main absorption bands in the XANES spectra.

199 ition, our calculations identify the exciton absorption bands in transient absorption spectra measure

200 rins showed large bathochromic shifts in the absorption bands, indicating that the electronic propert

201 tion into the p( perpendicular)(N)-->pi(N=C) absorption bands, indicating that the excited state is l

202 he dyes in a solution led to the increase in absorption band intensity in diffuse reflectance spectra

203 The lowest-energy absorption band is assigned as the transition from the a

204 The lowest energy absorption band is asymmetric with a weak low-energy sho

205 ysis revealed that the characteristic 695 nm absorption band is shifted to 687 nm and reversed after

206 In the present study, this absorption band is used to selectively resonance enhance

207 of nonplanar deformations on the UV-visible absorption bands is then probed experimentally with a se

208 The silver cluster has a single violet absorption band (lambda(max) = 400 nm), and its single-s

209 ne) that exhibits an intense long-wavelength absorption band (lambda(max) = 516 nm, epsilon(516) = 48

210 It is shown that irradiation at the main absorption band leads to cyclobutane dimers (T<>Ts) and

211 mu(eff) = 3.80 mu(B), and assignment of its absorption bands leads to the ligand field parameters De

212 e excellent electronic properties but narrow absorption bands limit their utility in certain optoelec

213 The SEIRA enhancement increases and the absorption band line shape becomes more asymmetric as th

214 sion on irradiation into the long-wavelength absorption bands localized on the porphyrin.

215 The radical-cations showed a broad absorption band located between 390 and 460 nm, while th

216 pper atom are either type 1, with an intense absorption band near 600 nm, or type 2, with weak absorp

217 nstrated remarkably red-shifted intense Q(y) absorption bands observed in the range of 816-850 nm wit

218 , the unique charge-resonance (intervalence) absorption bands observed upon the one-electron oxidatio

219 Absorption band of BODIPY was tuned by installation of 0

220 etramethylrhodamine shows the characteristic absorption band of dimers of rhodamine when KGlu is pres

221 sample absorbance is easily followed by the absorption band of localized surface plasmon resonance (

222 e at L135 and L247 shift the long-wavelength absorption band of P to higher energies.

223 We detected an absorption band of phenylborylene at 375 nm (S0 --> S2)

224 very intense surface plasmon resonance (SPR) absorption band of SNPs at 423 nm.

225 nches the fiber transmissions if there is an absorption band of the analyte overlapping with the tran

226 metallic nanoantennas tuned to a specific IR absorption band of the analyte to enhance the IR signal

227 tene overlaps almost perfectly with the Q(x) absorption band of the BChls.

228 sults in its eventual merge with the intense absorption band of the dye around 500 nm in 3-Resf.

229 roximately 250 M(-1) cm(-1)) charge-transfer absorption band of the HMS.Fe(II).HPP complex.

230 ained if the laser wavelength matches the UV absorption band of the matrix in the solid state well.

231 polymer backbone, so that the lowest optical absorption band of the polymer has considerable intramol

232 The broad absorption band of the QDs in the visible region offers

233 ansmission measurement that would lead to an absorption band of the same intensity, is a more accurat

234 induced CD at the surface plasmon resonance absorption band of the silver nanoparticles.

235 g of Cu ions, the strong near-infrared (NIR) absorption band of the starting CuS NCs was essentially

236 retical and experimental energy of the lower absorption band of these species.

237 ser flash photolysis experiments showing the absorption bands of 3-CN-NMQ(*) (lambdamax = 390 nm) and

238 significant changes in the characteristic IR absorption bands of all the bases and phosphate groups o

239 ecreasing the second transition enthalpy and absorption bands of amide I, II and III.

240 mposites exhibited broadened and red-shifted absorption bands of AuNRs in nIR region due to the plasm

241 rbance's as a function of time due to uv-vis absorption bands of both antioxidants and the enzymatic

242 ilbene chromophores has little effect on the absorption bands of capped hairpins.

243 is hindered by the superposition of similar absorption bands of carbonyl functional groups summing u

244 mbining data acquisition schemes to suppress absorption bands of H(2)O that overlap with the protein

245 erature range of 20-300 K as suggested by IR absorption bands of HOH bending and OH stretching modes

246 , time-resolved perturbations of the visible absorption bands of L29F and V68L deoxyMb generated afte

247 romic and hypsochromic shifts in the maximum absorption bands of MTX after interaction with DNA.

248 of DNA and the overlap of DNA bands with the absorption bands of other biochemical components.

249 the large red shifts seen in the UV-visible absorption bands of peripherally crowded nonplanar porph

250 3 is consistent with electrochromic shift of absorption bands of the Chl a pigments in the vicinity o

251 Independent VTVH-MCD studies on multiple absorption bands of the complex yield D = -14(3) cm(-1),

252 hemoglobin Soret absorption band and to the absorption bands of the dyes were used to demarcate the

253 orm disks with large linear dichroism in the absorption bands of the dyes.

254 resulting in a significant red shift of the absorption bands of the naphthalenic chromophore.

255 The absorption bands of the PA aliphatic backbone at 2902, 2

256 Dual absorption bands of the phenolic moiety indicate a doubl

257 emission of YFP and the visible-region (QX) absorption bands of the RC allow energy transfer via a F

258 The FTIR spectroscopy showed the absorption bands of the stretching modes of Zn-O between

259 Incidentally, the absorption bands of water increased resulting from surfa

260 n of nanosecond laser induced transient dual absorption bands, one in the bandgap (TA(1)) and another

261 However, their absorption bands provide limited coverage in the visible

262 can have (bacterio)chlorophyll Q(y) antenna absorption bands ranging from approximately 650 to appro

263 Their two-photon absorption bands reach into the NIR-II region of the ele

264 balamin at 520 nm in the low-lying alphabeta absorption band results in bond homolysis proceeding via

265 A large decrease in the FTIR absorption band's magnitude was observed in the hydrocar

266 le their fluorescence is overlapped with the absorption band(s) of the core metalloporphyrin, ensurin

267 The distinct origins of the absorption band shifts associated with the formation of

268 3d --> corrin pi* transitions and by visible absorption bands similar to the corrin pi-->pi* transiti

269 omic behavior of Ir(III)-corrole Soret and Q absorption bands suggests that the lowest singlet excite

270 Ar(4)(MeO)(8)TNPs exhibit more red-shifted absorption bands than Ar(4)TNPs and differ dramatically

271 O(-), and H2PO4(-) induced a new red-shifted absorption band that was attributed to a deprotonation p

272 The data shows a number of absorption bands that are assigned to one- and two-phono

273 In solution, 3a-c show strong disq--based absorption bands that are invariant across the halide se

274 s in length contained vestigial neutral (VN) absorption bands that arise from neutral parts of the ch

275 heir optical spectra: All show lowest energy absorption bands that correspond to an alpha-homo (highe

276 ndolines with varying basicities and tunable absorption bands that extend to the near-infrared region

277 eory of spectroscopy to fit the two observed absorption bands that have resolved vibronic structure.

278 spite the spectral red-shift of their lowest absorption band, the fluorescence quantum yields increas

279 By spectrum scanning at the -OH absorption band, the waveguide sensor was able to identi

280 Upon excitation into any of these four absorption bands, the (C(5)Me(5))(2)U[-N=C(Ph)(R)](2) co

281 citation into the lowest-energy ligand-field absorption band; the time constant is found to be indepe

282 l porphyrinoid photoproducts possess intense absorption bands throughout the visible spectral region,

283 witnessed by a strong red-shift of the probe absorption bands, thus allowing the generation of dichro

284 ieved by spectral matching of the sensitizer absorption band to different types of localized photon m

285 ene) to subppm amine contents turns on a new absorption band unambiguously ascribed to free bpee mole

286 tion constant and evaluation of intervalence absorption bands using appropriate theoretical models yi

287 Characteristic optical absorption bands, vibrational frequencies, and hyperfine

288 transfer character of the longest wavelength absorption band was confirmed.

289 Shifts in the absorption band wavelength and intensity as a function o

290 Shifts of 4-23 nm in the Q(y) absorption band were observed in seven mutants with sing

291 No new absorption bands were observed for either methionine or

292 P) can be excited at the red edge of the Trp absorption band which allows normalisation of the emissi

293 The caged compound has a major absorption band with a maximum at 390 nm (epsilon(390) =

294 The caged compound has a major absorption band with a maximum at 390 nm (epsilon390 = 1

295 we correlate a shift in the chlorophyll red absorption band with deformation of its tetrapyrrole mac

296 p-nitrophenyl phosphate, exhibits a visible absorption band with lambda(max) at 570 nm.

297 d LMCT excited state has a single CN-stretch absorption band with no anisotropy.

298 crocycles exhibited bathochromically shifted absorption bands with a distinct change in the color of

299 We detected prominent H2O absorption bands with a maximum base-to-peak amplitude o

300 ompounds and reveal at least two significant absorption bands within the region 420-550 nm.